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Author Details
Full Name
Joshua F McMichael
Affiliation
Washington University
ORCID
Career Start Year
2009
Papers
41
H Index
30
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37953380
DGIdb 5.0: rebuilding the drug-gene interaction database for precision medicine and drug discovery platforms.
Nucleic Acids Res
2024
37953380
DGIdb 5.0: rebuilding the drug-gene interaction database for precision medicine and drug discovery platforms.
Nucleic Acids Res
2024
36373660
CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.
Nucleic Acids Res
2023
36373660
CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.
Nucleic Acids Res
2023
37910143
Ultra-Deep Sequencing Reveals the Mutational Landscape of Classical Hodgkin Lymphoma.
Cancer Res Commun
2023
37027480
Computational prediction of MHC anchor locations guides neoantigen identification and prioritization.
Sci Immunol
2023
36949070
Integrated analysis of genomic and transcriptomic data for the discovery of splice-associated variants in cancer.
Nat Commun
2023
37910143
Ultra-Deep Sequencing Reveals the Mutational Landscape of Classical Hodgkin Lymphoma.
Cancer Res Commun
2023
36949070
Integrated analysis of genomic and transcriptomic data for the discovery of splice-associated variants in cancer.
Nat Commun
2023
37027480
Computational prediction of MHC anchor locations guides neoantigen identification and prioritization.
Sci Immunol
2023
35995947
Spatially restricted drivers and transitional cell populations cooperate with the microenvironment in untreated and chemo-resistant pancreatic cancer.
Nat Genet
2022
35444317
The Human Pangenome Project: a global resource to map genomic diversity.
Nature
2022
35624339
A community approach to the cancer-variant-interpretation bottleneck.
Nat Cancer
2022
35995947
Spatially restricted drivers and transitional cell populations cooperate with the microenvironment in untreated and chemo-resistant pancreatic cancer.
Nat Genet
2022
35444317
The Human Pangenome Project: a global resource to map genomic diversity.
Nature
2022
35624339
A community approach to the cancer-variant-interpretation bottleneck.
Nat Cancer
2022
33237278
Integration of the Drug-Gene Interaction Database (DGIdb 4.0) with open crowdsource efforts.
Nucleic Acids Res
2021
33963182
Co-evolution of tumor and immune cells during progression of multiple myeloma.
Nat Commun
2021
33577785
Proteogenomic and metabolomic characterization of human glioblastoma.
Cancer Cell
2021
33237278
Integration of the Drug-Gene Interaction Database (DGIdb 4.0) with open crowdsource efforts.
Nucleic Acids Res
2021
33577785
Proteogenomic and metabolomic characterization of human glioblastoma.
Cancer Cell
2021
33963182
Co-evolution of tumor and immune cells during progression of multiple myeloma.
Nat Commun
2021
31907209
pVACtools: A Computational Toolkit to Identify and Visualize Cancer Neoantigens.
Cancer Immunol Res
2020
31907209
pVACtools: A Computational Toolkit to Identify and Visualize Cancer Neoantigens.
Cancer Immunol Res
2020
31196969
Regulated Phosphosignaling Associated with Breast Cancer Subtypes and Druggability.
Mol Cell Proteomics
2019
31779674
Standard operating procedure for curation and clinical interpretation of variants in cancer.
Genome Med
2019
31196969
Regulated Phosphosignaling Associated with Breast Cancer Subtypes and Druggability.
Mol Cell Proteomics
2019
31779674
Standard operating procedure for curation and clinical interpretation of variants in cancer.
Genome Med
2019
29625052
Pathogenic Germline Variants in 10,389 Adult Cancers.
Cell
2018
30311370
Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards.
Hum Mutat
2018
30053901
Integrative omics analyses broaden treatment targets in human cancer.
Genome Med
2018
29625052
Pathogenic Germline Variants in 10,389 Adult Cancers.
Cell
2018
30053901
Integrative omics analyses broaden treatment targets in human cancer.
Genome Med
2018
30311370
Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards.
Hum Mutat
2018
28138153
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer.
Nat Genet
2017
28138153
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer.
Nat Genet
2017
27684579
DoCM: a database of curated mutations in cancer.
Nat Methods
2016
28389595
Cancer Immunogenomics: Computational Neoantigen Identification and Vaccine Design.
Cold Spring Harb Symp Quant Biol
2016
26657142
Systematic discovery of complex insertions and deletions in human cancers.
Nat Med
2016
26531824
DGIdb 2.0: mining clinically relevant drug-gene interactions.
Nucleic Acids Res
2016
27684579
DoCM: a database of curated mutations in cancer.
Nat Methods
2016
27821060
Visualizing tumor evolution with the fishplot package for R.
BMC Genomics
2016
28389595
Cancer Immunogenomics: Computational Neoantigen Identification and Vaccine Design.
Cold Spring Harb Symp Quant Biol
2016
26657142
Systematic discovery of complex insertions and deletions in human cancers.
Nat Med
2016
26531824
DGIdb 2.0: mining clinically relevant drug-gene interactions.
Nucleic Acids Res
2016
27821060
Visualizing tumor evolution with the fishplot package for R.
BMC Genomics
2016
26158448
Genome Modeling System: A Knowledge Management Platform for Genomics.
PLoS Comput Biol
2015
26645048
Optimizing cancer genome sequencing and analysis.
Cell Syst
2015
26158448
Genome Modeling System: A Knowledge Management Platform for Genomics.
PLoS Comput Biol
2015
26689913
Patterns and functional implications of rare germline variants across 12 cancer types.
Nat Commun
2015
1 - 50 of 82
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Michael N Edmonson
St. Jude Children's Research Hospital
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Rachel Karchin
Johns Hopkins University
Career Start Year
1998
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Adam Butler
Wellcome Sanger Institute
Career Start Year
1996
Number of shared co-authors
12
John V Pearson
QIMR Berghofer Medical Research Institute
Career Start Year
1996
Number of shared co-authors
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row(s) 1 - 30 of 30
Collaborators
Li Ding
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers
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Elaine R Mardis
The Ohio State University
Co-authored papers
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Obi L Griffith
Washington University
Co-authored papers
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Richard K Wilson
The Ohio State University
Co-authored papers
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Malachi Griffith
Washington University
Co-authored papers
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Christopher A Miller
Washington University School of Medicine
Co-authored papers
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Michael C Wendl
Washington University in St Louis
Co-authored papers
17
Robert S Fulton
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Co-authored papers
16
Timothy J Ley
Washington University School of Medicine
Co-authored papers
15
Michael D McLellan
McDonnell Genome Institute, Washington University in St. Louis
Co-authored papers
14
Jason Walker
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers
13
David E Larson
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers
13
Adam C Coffman
Washington University
Co-authored papers
12
Charles Lu
Co-authored papers
11
Daniel C Koboldt
Institute for Genomic Medicine, Nationwide Children's Hospital
Co-authored papers
10
Ken Chen
University of Texas MD Anderson Cancer Center
Co-authored papers
9
Lucinda Fulton
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers
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Alex H Wagner
Iowa State University, Mayo Clinic, Nationwide Children's Hospital, The Ohio State University College of Medicine, University of Iowa, Washington University in Saint Louis
Co-authored papers
9
Susanna Kiwala
Washington University
Co-authored papers
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Cyriac Kandoth
University of California los angeles
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John F DiPersio
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Feng Chen
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Matthew A Wyczalkowski
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Vincent Magrini
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James M Eldred
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